ClinVar Miner

Submissions for variant NM_001365999.1(SZT2):c.4480+4T>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000717552 SCV000848405 uncertain significance Seizures 2016-12-03 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence

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